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As a Clinical Research Associate, you will conduct and monitor clinical trials, ensure protocol compliance, and maintain data integrity while collaborating with site staff and investigators.

The Clinical Research Associate will conduct clinical trial visits, ensure protocol compliance, analyze data, and prepare study documentation while collaborating with site staff.

As a Clinical Research Associate, you will monitor clinical trials, ensure protocol compliance, and collaborate with investigators while analyzing medical data.

The Clinical Research Associate will design and analyze clinical trials, ensure protocol compliance, and maintain data integrity during studies.

As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.

Lead biostatistical components in clinical trials, oversee statistical activities, mentor junior statisticians, and ensure regulatory compliance.

The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

Oversee and manage clinical trial activities, ensuring compliance with protocols and regulations, while mentoring site staff and maintaining data integrity.

The Senior Clinical Research Associate oversees clinical trial activities, ensuring adherence to protocols and regulations while managing data integrity and participant safety throughout the study lifecycle.

The Senior Clinical Research Associate oversees clinical trial activities ensuring compliance with protocols and regulations, manages site performance, and trains staff.